RE: Mart-1 IHC- I need your expertise please!!
|From:||"Breckenridge, Richard A." |
We also use the same antibody from DAKO. We use the same procedure, except
we use DAB. We are also experiencing the same feedback from our
Dermatopathologist. The controls look great, but the patient's are not
staining as anticipated. You are not alone. We have a pic of our MART-1 on
our website.. www2.utmb.edu/pps Follow the SPECIAL PROCEDURES linkand click
on "Available Antibodies".
Richard A. Breckenridge HT(ASCP)
UTMB Special Procedures Laboratory
Clinical Sciences Building Room 504
Galveston, TX 77555-0748
Phone 409-772-8051 Fax 409-772-8030
From: Martha Ward [mailto:firstname.lastname@example.org]
Sent: Tuesday, April 01, 2003 8:20 AM
To: Vinnie Della Speranza; email@example.com
Subject: RE: Mart-1 IHC- I need your expertise please!!
I do not have an answer for any of Vinnie's questions except to say that I
have experienced the same thing and I would be interested in any feedback
that is generated.
Wake Forest University Baptist Medical Center
From: Vinnie Della Speranza [mailto:firstname.lastname@example.org]
Sent: Monday, March 31, 2003 4:45 PM
Subject: Mart-1 IHC- I need your expertise please!!
I'd appreciate any insight anyone may offer with the following.
we frequently perform Mart-1 ihc staining to demonstrate melanocytes. We use
a monoclonal antibody from Dako (clone A103 working dilution
1:50) for this marker and an alkaline phosphatase detection kit from
Biogenex utilizing a red chromogen. we perform high temperature antigen
retrieval in citrate buffer pH 6.0
our positive control is a nevus selected by one of our dermatopathologists.
we generally prepare a working dilution of this antibody once each week
from time to time, we've received feedback that "not enough melanocytes are
staining" which causes the dermpathologist to conclude that the antibody is
not performing to expectations. Slides are always checked prior to being
turned in to verify that we have achieved the expected pattern of staining,
however we do not attempt to quantitate the # of slides appearing positively
stained with this marker.
I reviewed a case today that had been rejected by the pathologist. In
evaluating the epidermis of four pieces of excised skin (FFPE), I found
evidence of appropriate staining in each, although some areas of the
epidermis contained many positive cells, some areas only a few, some areas
none at all. the melanocytes in our control nevus stained with the expected
pattern and intensity.
My questions to you are as follows:
has anyone found variable Mart-1 staining in tissues such as I've described
and if so, can you elaborate as to it's suspected cause?
is it possible that handling of the specimen prior to fixation and
processing could cause the result we are experiencing?
is it possible that pretreatment of the surgical site in the patient,
including the use of topical or injected anesthetics or skin disinfectants
could cause variable Mart-1 staining?
is there something about the stability of this antibody that we haven't
considered that may be contributing to this situation?
is it possible that the pathologist expected a different outcome and thus
concluded that the stain results were incorrect? your thoughts are most
Vinnie Della Speranza
Manager for Anatomic Pathology Services
Medical University of South Carolina
165 Ashley Avenue Suite 309
Charleston, SC 29425
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